Canonical Allele Identifier: CA1396723585
Gene: NR1I2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119807563A= , CM000665.2:g.119807563A= GRCh38
NC_000003.11:g.119526410A= , CM000665.1:g.119526410A= GRCh37
NC_000003.10:g.121009100A= NCBI36
NG_011856.1:g.32080A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393716.8:c.197+116A= MANE Select ENSP00000377319.3:n.197+116A=
ENST00000466380.6:c.197+116A= ENSP00000420297.2:n.197+116A=
ENST00000648112.1:c.*336A= ENSP00000497876.1:n.*336A=
ENST00000337940.4:c.314+116A= ENSP00000336528.4:n.314+116A=
ENST00000393716.6:c.197+116A= ENSP00000377319.2:n.197+116A=
ENST00000466380.5:c.197+116A= ENSP00000420297.1:n.197+116A=
ENST00000474090.1:n.485+116A=
NM_003889.3:c.197+116A= NP_003880.3:n.197+116A=
NM_022002.2:c.314+116A= NP_071285.1:n.314+116A=
NM_033013.2:c.197+116A= NP_148934.1:n.197+116A=
NM_003889.4:c.197+116A= MANE Select NP_003880.3:n.197+116A=
NM_022002.3:c.314+116A= NP_071285.1:n.314+116A=
NM_033013.3:c.197+116A= NP_148934.1:n.197+116A=
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